HYDROLYTIC STABILITY OF IMIDES OF DIFFERENT STRUCTURES
Abstract
The conversion kinetics of N(o-carboxyphenyl)naphthalimide has been studied in buffer solutions over a pH range 5-12.6 and temperature range 25-70 °C. The naphthalimide hydrolysis is shown to be a reversible reaction. The mechanism of the alkaline hydrolysis of N(o- carboxyphenyl) phthalimide is proposed. The structure dependence of the imide hydrolytic stability is explained on the basis of the suggested mechanism.
How to Cite
Donskikh, A. I., Tseitlin, G. M., Tomina, O. I., Saikina, Z. F., Doroshenko, J. E. “HYDROLYTIC STABILITY OF IMIDES OF DIFFERENT STRUCTURES ”, Periodica Polytechnica Chemical Engineering, 33(1), pp. 61–67, 1989.
Issue
Section
Articles